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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4418236copy number variation1nstd174human GRCh37 chr9: 35,662,900-35,664,584 , GRCh38.p12 chr9: 35,662,903-35,664,587 ARHGEF39
    esv3620382copy number variation8estd214human GRCh37 chr9: 35,662,893-35,664,514 , GRCh38.p12 chr9: 35,662,896-35,664,517 ARHGEF39

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